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70 results for “hind wing”
FIGURE 29. Cloeodes xyrognathos, male imago. a. Fore wing. b. Hind wing. d. Hind wing, enlarged. d in Revealing the diversity of Cloeodes Traver, 1938 (Ephemeroptera: Baetidae) in the Neotropics: description of eleven new species from Brazilian mountain ranges
FIGURE 29. Cloeodes xyrognathos, male imago. a. Fore wing. b. Hind wing. d. Hind wing, enlarged. d. Genitalia.
FIGURE 10. Cloeodes amantykyra, male imago. a. Fore wing. b. Hind wing. c in Revealing the diversity of Cloeodes Traver, 1938 (Ephemeroptera: Baetidae) in the Neotropics: description of eleven new species from Brazilian mountain ranges
FIGURE 10. Cloeodes amantykyra, male imago. a. Fore wing. b. Hind wing. c. Hind wing (enlarged). d. Genitalia (fbforceps base, fsi to fsiii—forceps segment I to III).
FIGURE 28–30. Dimophora parva n. sp., ♀ holotype. 28, Fore wing; 29, hind wing; 30, axilla, scutellum, metanotum and propodeum in dorsal view. Scale lines, 0.5mm for 28, 29; 0.2mm for 30. in Revision of the genus Dimophora Förster (Hymenoptera: Ichneumonidae: Cremastinae) from Japan
FIGURE 28–30. Dimophora parva n. sp., ♀ holotype. 28, Fore wing; 29, hind wing; 30, axilla, scutellum, metanotum and propodeum in dorsal view. Scale lines, 0.5mm for 28, 29; 0.2mm for 30.
FIGURE 16–18. Dimophora nigra n. sp., ♀ holotype. 16, Fore wing; 17, hind wing; 18, axilla, scutellum, metanotum and propodeum in dorsal view. Scale lines, 0.5 mm for 16, 17; 0.2 mm for 18. in Revision of the genus Dimophora Förster (Hymenoptera: Ichneumonidae: Cremastinae) from Japan
FIGURE 16–18. Dimophora nigra n. sp., ♀ holotype. 16, Fore wing; 17, hind wing; 18, axilla, scutellum, metanotum and propodeum in dorsal view. Scale lines, 0.5 mm for 16, 17; 0.2 mm for 18.
FIGURE 7–9. Dimophora japonica n. sp., ♀ holotype. 7, Fore wing; 8, hind wing; 9, axilla, scutellum, metanotum and propodeum in dorsal view. Scale lines, 0.5 mm for 7, 8; 0.2 mm for 9. in Revision of the genus Dimophora Förster (Hymenoptera: Ichneumonidae: Cremastinae) from Japan
FIGURE 7–9. Dimophora japonica n. sp., ♀ holotype. 7, Fore wing; 8, hind wing; 9, axilla, scutellum, metanotum and propodeum in dorsal view. Scale lines, 0.5 mm for 7, 8; 0.2 mm for 9.
FIGURE 6. A Hind wing, P in Taxonomic revision of the genus Parena Motschulsky, 1860 (Coleoptera, Carabidae, Lebiini, Metallicina)
FIGURE 6. A Hind wing, P. (Crossoglossa) cavipennis (Bates), Beijing, scale bar = 1mm. Abbreviations: oc oblongum cell; wc wedge cell. B–G Tarsals claws of right hindlegs for Metallicina spp., scale bar = 0.2mm: B Pachycallida rufoplagiata Jeannel, Madagascar, Sept Lacs, female. C Metallica viridipennis Chaudoir, Cameroon, Bois des Singes, male. D P. (Crossoglossa) sciakyi sp. n., holotype. E P. (Bothynoptera) kurosai Habu, Nepal. F P. (Bothynoptera) heteronycha sp. n., Laos, paratype. G P. (Parena) latecincta (Bates), Vietnam. H Protibia of P. (Parena) nigrolineata (Chaudoir), scale bar = 0.5 mm. I Mesotarsomeres of male of P. (Parena) nigrolineata (Chaudoir), adhesive hairs present on mesotarsomere 1, scale bar = 0.2mm. J Mesotarsomeres of male for P. (Parena) latecincta (Bates), adhesive hairs absent from mesotarsomere 1, scale bar = 0.2mm.
FIGURE 3. Hind wing. a in Two new species of Clavicornaltica Scherer (Coleoptera, Chrysomelidae, Galerucinae) from the Ryukyu Islands, Southwestern Japan, with a redescription of C. sakishimana Suenaga and Yoshida
FIGURE 3. Hind wing. a, Clavicornaltica sakishimana, male (HS-22-8); b, ditto, female (HS-22-4); c, C. tokushigei sp. nov. (HS-22-9); d, C. nakanoi sp. nov. (HS-22-12).
Figs. 22–23. Hind wing veination. 22 in New Species Of The Genus Oronoqua Fennah (Hemiptera: Auchenorrhyncha: Fulgoroidea: Issidae) From Inland Ecuador
Figs. 22–23. Hind wing veination. 22, Oronoqua
Fig. 11. Meru phyllisae, hind wing. A in A new aquatic beetle family, Meruidae, from Venezuela (Coleoptera: Adephaga)
Fig. 11. Meru phyllisae, hind wing. A, Brachypterous condition; B, macropterous condition.
Supplementary material 3 from: Ren J, Bai M, Yang X-K, Zhang R-Z, Ge S-Q (2017) Geometric morphometrics analysis of the hind wing of leaf beetles: proximal and distal parts are separate modules. ZooKeys 685: 131-149. https://doi.org/10.3897/zookeys.685.13084
Coordinates data of landmarks. :
Figure 4 from: Ren J, Bai M, Yang X-K, Zhang R-Z, Ge S-Q (2017) Geometric morphometrics analysis of the hind wing of leaf beetles: proximal and distal parts are separate modules. ZooKeys 685: 131-149. https://doi.org/10.3897/zookeys.685.13084
Figure 4 - Modularity test results. A The hypothesized partition: proximal part landmarks 1-6, 23, 24, and 26–36 and distal part landmarks 7–22, 25; different colour presents different modules B The partition with minimal covariance in all evaluated 104 partitions by RV coefficient C The partition with minimal covariance in all evaluated 106 partitions by RV coefficient.
Figure 2 from: Ren J, Bai M, Yang X-K, Zhang R-Z, Ge S-Q (2017) Geometric morphometrics analysis of the hind wing of leaf beetles: proximal and distal parts are separate modules. ZooKeys 685: 131-149. https://doi.org/10.3897/zookeys.685.13084
Figure 2 - PCA and CVA results. A Centroid size graph of hind wing landmarks (Procrustes fit) B PCA results, the shape changes associated with the first three PCs: the relative size of the apical area which could be considered the main feature (variance contribution ratio was 45.01%) to influence of the overall variance of the hind wing, the changes of cross vein cv in the middle area (variance contribution ratio was 12.39%), and relative size of the anal area size (variance contribution ratio was 10.56%) C CVA results, the axis of CV1 and CV2 presented the first two large shape variance of all variance; points with different colours indicated different subtribes' specimens; the ellipse is presented as an equal-frequency ellipse with a given probability level of 90%, which contains approximately 90% of the data points.
Figure 1 from: Ren J, Bai M, Yang X-K, Zhang R-Z, Ge S-Q (2017) Geometric morphometrics analysis of the hind wing of leaf beetles: proximal and distal parts are separate modules. ZooKeys 685: 131-149. https://doi.org/10.3897/zookeys.685.13084
Figure 1 - Leaf beetle hind wing (Chrysomela populi Linnaeus), with landmark locations (the dot with number), vein nomenclature and regional division. The nomenclature of the wing venation follows that of Kukalová-Peck & Lawrence (1993, 2004). Radial area: green, central area: blue, medial area: purple, anal area: yellow, apical (folding) area: red. Proximal part landmarks 1–6, 23, 24, and 26–36 mainly include radial, medial, and anal areas; distal part landmarks 7–22 and 25 include the central area, radial cell, and apical area. Abbreviations: Costa (C), Subcosta (Sc), Subcosta Anterior (ScA), Subcosta Posterior (ScP), Radius Anterior (RA), Radius Posterior (RP), Radial cross veins (r3, r4), Media Posterior (MP), Radio-medial cross veins (rp-mp1, rp-mp2), medial cross vein (cv), Cubitus Anterior (CuA), Medio-cubital Cross-vein or Arculus (mp-cua), Anal Anterior (AA), Anal posterior (AP). "+" indicates fused veins. The sub-number of veins reflects vein branches.
Figure 3 from: Ren J, Bai M, Yang X-K, Zhang R-Z, Ge S-Q (2017) Geometric morphometrics analysis of the hind wing of leaf beetles: proximal and distal parts are separate modules. ZooKeys 685: 131-149. https://doi.org/10.3897/zookeys.685.13084
Figure 3 - PLS analysis results. A Scatter plot of the PLS1 of two blocks B Shape changes associated with the first PLS axes of two blocks: each diagram shows the block change along the PLS1 in the positive or negative direction, corresponding to Figure 3A.
Fig. 1 in Phylogenomics and deep convergence in cockroach hind-wing morphology
Fig. 1 Phylogeny of Blattodea (a) and wing morphology illustration (b). a The phylogeny presented is the final species tree resulting from a number of topology tests and inference methods (IQ-TREE and ASTRAL). Node support values represent bootstrap frequency (3000 replicates from concatenation analyses of all three modified alignments; left) and gene concordance factors among the 41 loci (right). Taxa in bold have hind wings with a very large apical folding area (b – i, and b – ii). The apical region in Diploptera may not be homologous to those of other taxa so we use another symbol and did not count them as addi-
FIGURES 12–13. Fowlerium spp., hind wing. 12—F in To the revision of the genus Thionia Stål (Hemiptera, Fulgoroidea, Issidae), with description of new genera and new subtribe
FIGURES 12–13. Fowlerium spp., hind wing. 12—F. naso (Fowler); 13—F. productum (Van Duzee).
Figure 2 from: Guan K, Su J, Wang J, Yang Y (2015) Significance of hind wing morphology in distinguishing genera and species of cantharid beetles with a geometric morphometric analysis. ZooKeys 502: 11-25. https://doi.org/10.3897/zookeys.502.9191
Figure 2 - Shape variables of the hind wings in the genera of Lycocerus, Prothemus and Themus. A principal component analysis (PCA) of hind wing configuration. Plot of PC1 (74.39% of total variation) and PC2 (8.52% variation) showing 90% confidence ellipses of population means B canonical variate analysis (CVA) of same matrix, also showing 90% confidence ellipses of population means. The averaged shape of each genus is depicted as deformations using thin plate splines.
Figure 5 from: Guan K, Su J, Wang J, Yang Y (2015) Significance of hind wing morphology in distinguishing genera and species of cantharid beetles with a geometric morphometric analysis. ZooKeys 502: 11-25. https://doi.org/10.3897/zookeys.502.9191
Figure 5 - Shape variables of the hind wings in the Themus species. A principal component analysis (PCA) of hind wing configuration. Plot of PC1 (32.87% of total variation) and PC2 (16.48% variation) showing 90% confidence ellipses of population means B canonical variate analysis (CVA) of same matrix, also showing 90% confidence ellipses of population means. The averaged shape of each species is depicted as deformations using thin plate splines.
Figure 4 from: Guan K, Su J, Wang J, Yang Y (2015) Significance of hind wing morphology in distinguishing genera and species of cantharid beetles with a geometric morphometric analysis. ZooKeys 502: 11-25. https://doi.org/10.3897/zookeys.502.9191
Figure 4 - Shape variables of the hind wings in the Prothemus species. A principal component analysis (PCA) of hind wing configuration. Plot of PC1 (38.40% of total variation) and PC2 (15.88% variation) showing 90% confidence ellipses of population means B canonical variate analysis (CVA) of same matrix, also showing 90% confidence ellipses of population means. The averaged shape of each species is depicted as deformations using thin plate splines.
Figure 3 from: Guan K, Su J, Wang J, Yang Y (2015) Significance of hind wing morphology in distinguishing genera and species of cantharid beetles with a geometric morphometric analysis. ZooKeys 502: 11-25. https://doi.org/10.3897/zookeys.502.9191
Figure 3 - Shape variables of the hind wings in the Lycocerus species. A principal component analysis (PCA) of hind wing configuration. Plot of PC1 (49.02% of total variation) and PC2 (14.92% variation) showing 90% confidence ellipses of population means B canonical variate analysis (CVA) of same matrix, also showing 90% confidence ellipses of population means. The averaged shape of each species is depicted as deformations using thin plate splines.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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